Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/2058

TitlePalladium-catalyzed borylation and Suzuki coupling (BSC) to obtain beta-substituted dehydroamino acid derivatives
Author(s)Abreu, Ana S.
Silva, Natália O.
Ferreira, Paula M. T.
Queiroz, Maria João R. P.
KeywordsBenzo[b]thiophenes
Borylation
Palladium
Suzuki coupling
Dehydroamino acids
Issue date2003
PublisherElsevier
JournalTetrahedron Letters
Citation"Tetrahedron letters". 44 (2003) 6007-6009.
Abstract(s)Several benzo[b]thienyldehydroamino acids were prepared by one pot palladium-catalyzed borylation and Suzuki coupling (BSC) from bromobenzo[b]thiophenes containing EDG (OMe or Me), as the component to be borylated with pinacolborane, and pure stereoisomers of beta-bromodehydroamino acid derivatives. To our knowledge it is the first time that the BSC reaction involves a non aromatic system.
TypeArticle
URIhttp://hdl.handle.net/1822/2058
DOI10.1016/S0040-4039(03)01473-4
ISSN0040-4039
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CDQuim - Artigos (Papers)

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